Process for preparing a compound useful in preparing ace inhibitors and intermediate produced thereby

ABSTRACT

A compound (for preparing an ACE inhibitor), namely, triphenyl cerium and a process for preparing same by reacting cerium trichloride (CeCl 3 ) with phenyllithium, are provided.

This is a division of application Ser. No. 44,691, filed May, 1987, nowU.S. Pat. No. 4,734,508.

FIELD OF THE INVENTION

The present invention relates to a process for preparing(cis)-4-hydroxy-4-phenyl-L-proline derivatives which are novelintermediates in the preparation of trans-4-substituted-L-prolines and,which in turn, are useful as intermediates in the preparation of certainangiotensin-converting enzyme (ACE) inhibitors.

DESCRIPTION OF THE INVENTION

In accordance with the present invention, a process is provided forpreparing (cis)-4-hydroxy-4-phenyl-L-proline derivatives of thestructure I ##STR1## wherein R₁ is a nitrogen protecting group such asbenzoyl, benzyloxycarbonyl, t-butoxycarbonyl, benzene sulfonyl, toluenesulfonyl, benzyl, benzhydryl, trityl, acetyl, trifluoroacetyl and thelike, and X is OR₂ where R₂ is hydrogen or an acid protecting group suchas lower alkyl, phenyl-lower alkyl or a metal ion such as Na, K or Li,or X is NR₃ R₄ wherein R₃ and R₄ may be the same or different and arehydrogen, lower alkyl, aryl or arylalkyl or R₃ and R₄ together with theN to which they are attached form a 5-, 6- or 7-membered ring such as##STR2##

The process of the invention includes the step of reactingtriphenylcerium

    (C.sub.6 H.sub.5).sub.3 Ce

with the 4-ketopropline derivative III ##STR3## in the presence of aninert organic solvent such as tetrahydrofuran, ether, toluene or dioxaneor a mixture of two or more thereof, at reduced temperatures of fromabout -90° C. to about -10° C. and preferably from about -80° C. toabout -50° C., for a period of from about 0.5 to about 6 hours andpreferably from about 0.5 to about 2 hours to form the prolinederivative I.

In carrying out the above invention, the keto compound III will beemployed in a molar ratio to the triphenylcerium compound II as set outbelow ##STR4## where in keto compound III, X is OH, then III is employedin a molar ratio to II of within the range of from about 2.5:1 to about1:1 and preferably from about 2.2:1 to about 1.2:1; where in ketocompound III, X is Oalkyl, then III is employed in a molar ratio to IIof within the range of from about 4:1 to about 2:1 and preferably fromabout 3.5:1 to about 2.5:1, where in keto compound III, X is ##STR5##then III is employed in a molar ratio to II of within the range of fromabout 4:1 to about 2:1 and preferably from about 3.5:1 to about 2.5:1;where in keto compound III, X is NR₃ R₄, then III is employed in a molarratio to II of within the range of from about 2.5:1 to about 1:1 andpreferably from about 2.2:1 to about 1.2:1; and where in compound III, Xis Ometal ion such as ONa, then III is employed in a molar ratio to IIof within the range of from about 4:1 to about 2:1 and preferably fromabout 3.5:1 to about 2.5:1.

The (cis)-4-hydroxy-4-phenyl proline derivative I may then be employedto form a (trans)-4-phenyl-L-proline derivatives IV of the structure##STR6## by treating the (cis)-4-hydroxy-4-phenyl proline derivatives Iwith a dehydrating agent such as p-toluenesulfonic acid in the presenceof acetic anhydride, or any other dehydrating agent such as TFA(trifluoroacetic acid), BF₃ O(Et)₂ (boron trifluoride etherate), methanesulfonyl chloride and triethylamine or refluxing with p-toluenesulfonicacid in an inert solvent such as methylene chloride, chloroform, tolueneor tetrahydrofuran, employing a molar ratio of proline I:dehydratingagent of within the range of from about 0.1:1 to about 10:1, to form theprotected compound acid ##STR7## which is treated with reducing agentsuch as an alkali or alkaline earth metal such as lithium, potassium,sodium, calcium and the like and ammonia employing a molar ratio ofV:reducing agent of within the range of from about 0.25:1 to about0.07:1 and preferably from about 0.2:1 to about 0.1:1, in the presenceof an inert organic solvent such as tetrahydrofuran, to reduce thedouble bond and to remove the nitrogen protecting group and/or acidprotecting group (if present) to form the acid IV. Where an acidprotecting group X is also present then additional reducing agent willbe employed to provide a molar ratio of V:reducing agent of within therange of from about 0.25:1 to about 0.1:1, and preferably from about0.2:1 to about 0.15:1.

The phenyl proline derivative IV may be employed to form thecorresponding trans-4-cyclohexyl-L-proline of the structure ##STR8## byreducing compound IV using, for example, hydrogen in the presence of acatalyst such as platinum, rhodium or other reducing catalyst.

In another embodiment, compounds of the formula VI can be directlyprepared from compounds of the formula V as follows. Compound V isexhaustively reduced by treatment with an alkali or alkaline earth metalsuch as lithium, potassium, sodium, calcium and the like in the presenceof an alcohol solvent such as ethanol or methanol, in liquid ammonia, toproduce a compound of the formula VII ##STR9## which is converted tocompound VI by catalytic hydrogenation methods such as hydrogenating VIIin the presence of a catalyst such as palladium, rhodium or otherhydrogenation catatlyst.

The 4-substituted proline derivative IV may be employed to formangiotensin converting enzyme inhibitors as described in U.S. Pat. No.4,337,201 to Petrillo.

The above Petrillo patent covers the following antiotensin-convertingenzyme inhibitor which is also referred to as fosinopril. ##STR10##

Listed below are definitions of the terms used in this specification.These definitions apply to the terms as they are used throughout thespecification (unless they are otherwise limited in specific instances),either individually or as part of a larger group.

The terms "alkyl" and "alkoxy" refer to both straight and branched chaingroups. Those groups having 1 to 10 carbon atoms are preferred.

The terms "cycloalkyl" and "cycloalkenyl" refer to groups having 3 to 7carbon atoms.

The term "aryl" refers to phenyl or phenyl substituted with halogen,alkyl, alkoxy, alkylthio, hydroxy, alkanoyl, nitro, amino, dialkylamino,or trifluoromethyl groups.

The term "alkanoyl" refers to groups having 2 to 9 carbon atoms.

The term "halogen" refers to fluorine, chlorine, bromine and iodine.

The 4-ketoproline derivatives III are known compounds and may beprepared as described by Patchett et al, "Studies on Hydroxyproline",J.A.C.S. 79, 185 (1957) and by Mauger et al, Chem. Rev. 66, 47 (1966).

The triphenylcerium compound II is a novel compound and may be preparedby reacting a solution of cerium trichloride

    CeCl.sub.3 A

in an inert organic solvent such as hexane, ether, tetrahydrofuran,toluene or a mixture of two or more thereof, with a solution ofphenyllithium

    C.sub.6 H.sub.5 Li B

in an inert organic solvent such as hexane, ether, tetrahydrofuran,toluene or the like, at a temperature within the range of from about-90° C. to about -10° C. and preferably from about -80 to about -50° C.,for a period of from about 0.1 to about 3 hours and preferably fromabout 0.2 to about 1 hour, employing a molar ratio of A:B of within therange of from about 0.2:1 to about 1:1 and preferably from about 0.25:1to about 0.35:1.

Examples of 4-keto proline derivatives III useful as starting materialsin carrying out the process of the invention include, but are notlimited to, the following.

    ______________________________________                                         ##STR11##                                                                    R.sub.1              X                                                        ______________________________________                                         ##STR12##           OH                                                        ##STR13##           CH.sub.3 O                                                ##STR14##           C.sub.6 H.sub.5 CH.sub.2 O                               C.sub.6 H.sub.5 CH.sub.2                                                                           C.sub.6 H.sub.5 CH.sub.2 O                               (C.sub.6 H.sub.5).sub.2 CH                                                                         C.sub.2 H.sub.5 O                                        (C.sub.6 H.sub.5).sub.3 C                                                                          CH.sub.3 O                                                ##STR15##           OH                                                        ##STR16##           NHCH.sub.3                                               C.sub.6 H.sub.5 CH.sub.2                                                                           NH.sub.2                                                 (C.sub.6 H.sub.5).sub.2 CH                                                                         N(C.sub.2 H.sub.5).sub.2                                  ##STR17##                                                                                          ##STR18##                                               (C.sub.6 H.sub.5).sub.3 C                                                                           ##STR19##                                                ##STR20##           OH                                                        ##STR21##           CH.sub.3 O                                                ##STR22##           CH.sub.3 O                                                ##STR23##           OH                                                        ##STR24##           CH.sub.3 O                                                ##STR25##                                                                                          ##STR26##                                                ##STR27##           OH                                                       ______________________________________                                    

The following working Examples represent preferred embodiments of thepresent invention. Unless otherwise indicated, all temperatures areexpressed in degrees Centigrade.

EXAMPLE 1 Triphenylcerium

A 4-necked 500 ml flask was equipped with a mechanical stirrer, argoninlet, low temperature (-78° C.) thermometer and a septem cap. 250 mldried tetrahydrofuran was added to the flask. 34.4 g (0.14 mol)anhydrous CeCl₃ was added to the tetrahydrofuran with vigorous stirringand stirring was continued for 2 hours at room temperature. A yellowishorange suspension formed which was cooled to -78° C. Phenyllithium(197.7 ml, 0.38 mol) in hexane-ether was added via a syringe through thespetum cap with vigorous stirring while the internal temperature wasmaintained at about -70° C. The initial yellow suspension changed colorto white, then yellow, then orange and finally to a red solution. Thered solution which was stirred for 30 minutes at -75° C. contained titlecompound and was employed as a reactant in Example 2.

EXAMPLE 2(cis)-4-Hydroxy-4-phenyl-1-[(phenylmethoxy)-carbonyl]-L-proline

A 4-necked 1 liter flask was equipped with a mechanical stirrer, argoninlet, low temperature (-78° C.) thermometer and a septum cap. 200 mldried tetrahydrofuran was added to the flask. Thereafter,4-keto-1[(phenylmethoxy)carbonyl]-L-proline (50.0 g, 0.19 mol) was addedto the tetrahydrofuran, the mixture was stirred to dissolve solids, andwas cooled to -78° C. The red solution of triphenylcerium prepared inExample 1 was added via a double ended needle with vigorous stirringwhile maintaining the internal temperature at -70° C. The solution wasstirred for 5 minutes at -78° C. while checking the TLC for completereaction. 50 ml hydrochloric acid (1:1 conc. acid:water) was added withvigorous stirring and most of (not all) of the tetrahydrofuran wasremoved on a rotavap at ˜40° C. The remaining concentrate was dilutedwith water, if necessary pH was adjusted to 1 with HC1, and the mixtureextracted with ethyl acetate (3×200 ml). The combined organic phase waswashed with HCl (1×100 ml, 1:1) and water (1×200 ml). The organic phasewas extracted with saturated sodium bicarbonate solution (5×100 ml) andthe combined sodium bicarbonate solution was back extracted once withethyl acetate. The sodium bicarbonate solution was diluted with 250 mlethyl acetate and acidified with vigorous stirring using concentratedhydrochloric acid. The layers were separated, the aqueous phase wasextracted with ethyl acetate (3×200 ml), the combined organic phasewashed with saturated sodium bisulfite solution (2×100 ml), the organicphase washed with water and brine, and dried over anhydrous MgSO₄, andthe solvent evaporated on a rotavap to give a thick gum residue. Theresidue was dissolved in 40 ml ethyl acetate and the mixture was dilutedwith 50 ml hexane to a slight turbidity at room temperature and thenseeded with crystals. After a few hours, the mixture was kept in a coldroom overnight, filtered, washed with 30% ethyl acetate in hexane(ice-cold) and with hexane. The solids were air dried to give 46.7 g oftitle compound, m.p. 122°-126° C. α_(D) =-50° (c=1, CHCl₃).

EXAMPLE 3 4-Phenyl-1-[(phenylmethoxy)carbonyl]-3,4-dehydro-L-proline

The Example 2 proline compound (1 g, 0.003 mol) was combined withp-toluenesulfonic acid (0.56 g, 0.003 mol), in methylene chloride (20ml) and the mixture was stirred for 5 minutes. Acetic anhydride (0.34 g,0.0033 mol, 0.32 ml) was added and the mixture was stirred for 1 hour atroom temperature to form a clear to slightly yellow solution. TLC showedthat the reaction was almost complete. An additional 0.1 ml aceticanhydride was added and the reaction was allowed to proceed anadditional 1 hour. TLC showed that the reaction was complete.

The methylene chloride was evaporated, the residue was reconstitutedwith ethyl acetate, washed with brine 5 times, dried (MgSO₄), filteredand evaporated to give 930 mg crude solid. The solid was recrystallizedfrom ethyl acetate/hexane to yield 0.772 g, 79.6%, m.p. 154°-155° C.

EXAMPLE 4

(trans)-4-Phenyl-L-proline

Example 3 acid compound (20 g, 0.062 mol) in 40 ml tetrahydrofuran wasadded to a solution of lithium (3.03 g, 0.433 mol, 7 eq) and ammonia(2.5 l) (with 30 minutes of stirring) and tetrahydrofuran (2 l). Afterthe addition, the reaction mixture was stirred for 40 minutes at -78° C.and quenched with ammonium chloride. Ammonia was evaporated at roomtemperature overnight. Tetrahydrofuran was evaporated, the solid residuewas suspended in water and acidified with HC1 to pH 1. The mixture wasconcentrated to 250 ml during which time some crystals formed. The pHwas brought to 6.3 by addition of NaOH and left at room temperatureovernight. The mixture was filtered, washed with water (2×50 ml, icecold) and acetonitrile (2×150 ml) and hexane, air dried overnight toyield 11.8 g (100%) of title product. HPLC: cis-6.1%, trans 93.9%, ratio15.4:1

Analyses: C₁₁ H₁₃ O₂ N

Calcd: C, 69.01; H, 6.85; N, 7.33.

KF 6.5% H₂ O, 0.74 moles: C, 64.50, H, 7.13: N, 6.85

Found: C, 64.69; H, 6.95; N, 7.29

[α]_(D) =+19.7° (c=1, 1N HCl)

EXAMPLE 5(cis)-4-Hydroxy-4-phenyl-1-[(phenylmethoxy)carbonyl]-L-pyroline-pyrrolidineamide A. 4-Keto-1-[(phenylmethoxy)carbonyl]carbonyl]-L-prolinepyrrolidine amide

To a solution of 10 g (0.0377 mol) of4-keto-1-[(phenylmethoxy)carbonyl]-L-proline in 200 ml methylenechloride was added 6.35 g (0.0415 mol) hydroxybenzotriazole. The mixturewas cooled to 0° C., dicyclohexylcarbodiimide (87 g) added and themixture was stirred at room temperature for 2 hours. The mixture wascooled to 0° C. and pyrrolidine (3.2 ml) added. The cooling bath wasremoved and the mixture was stirred at room temperature for 12 hours.The mixture was then cooled in an ice bath, acidified with 20% HCl to pH2, filtered, washed with NaHCO₃ and HCl. Normal workup produced thetitle compound which was crystallized from ethyl acetate-hexane to yield9.5 g, m.p. 109°-111° C.

B.(cis)-4-Hydroxy-4-phenyl-1-[(phenylmethoxy)carbonyl]-L-prolinepyrrolidineamide

Triphenylcerium prepared as in Example 1 [from 12.87 g of CeCl₃ and 49ml of PhLi]was added to a solution of the Part A keto-amide [30.0 g in150 ml THF]with vigorous stirring at ˜-75° C. After the reaction, usualwork up followed by crystallization produced the title compound in 78%(29.0 g) yield, m.p. 136°-138° C.

EXAMPLE 6 4-Phenyl-1-[(phenylmethoxy)carbonyl]-3,4-dehydro-L-prolinepyrrolidine amide

Following the procedure of Example 3, except substituting the prolinecompound of Example 5B for the proline compound of Example 2, the titlecompound was obtained.

EXAMPLE 7 (cis)-4-Hydroxy-4-phenyl-1-[(phenylmethoxy)carbonyl]-L-prolinebenzyl ester A. 4-Keto-1-[(phenylmethoxy)carbonyl]-L-proline benzylester

5 g (0.02 mmol) of 4-keto-1-[(phenylmethoxy)carbonyl]-L-proline wasdissolved in 50 ml dimethylformamide, 2.62 ml (0.022 mmol) of benzylbromide and 3.59 g (0.026 mmol) of potassium carbonate were added. Thereaction mixture was stirred for 1 hour followed by normal extractivework to give the title compound, 3.5 gm (49% yield), m.p. 55°-56° C.

[α]_(D) =-6° (c=1, CHCl₃)

B. (cis)-4-Hydroxy-4-phenyl-1-[(phenylmethoxy)carbonyl)]-L-proline

benzyl ester

Triphenyl cerium prepared as in Example 1 [from 3.1 g of CelCl₃ and11.78 ml of phenyllithium] was added to a solution of the Part Aketo-ester (8.0 g in 40 ml THF] with vigorous stirring and cooling (-78°C.). After this addition, the reaction was quenched with 25% HCl acidand followed by usual extractive workup and crystallization to give thetitle compound in 77.8% (7.6 gm) yield.

EXAMPLE 8 (cis)-4-Hydroxy-4-phenyl-1-(benzoyl)-L-proline

Triphenylcerium prepared as in Example 1 [from 23.4 g CeCl₃ and 102 mlphenyllithium]was added to a solution of the keto acid (20 g in 140 mlTHF) with vigorous stirring and cooling. After the addition, thereaction was stirred from 30 minutes at -78° C., quenched with 25% HClacid and work up as usual to get the crude material which wascrystallized from ethyl acetate to produce 17.0 g (64%) of the titlematerial as white crystals.

EXAMPLE 9 4-phenyl-1-(benzoyl)-3,4-dehydro-L-proline

Following the procedure as described in Example 3 except substitutingthe Example 8 proline compound for the Example 2 proline compound, thetitle compound was obtained.

Example 10 (trans)-4-Phenyl-L-proline

The procedure of Example 4 was followed except that the Example 9compound was used as the starting material. Thus, a solution of 2.0 g(0.0068 moles) of the dehydro-proline in 25 ml THF was added to asolution of lithium (0.33 g, 0.478 moles) in ammonia (300 ml) and THF(200 ml) at ˜-78° C. After the addition, the reaction mixture wasstirred for 20 minutes at -78° C., quenched with 2.0 g ammonium chlorideand worked up as in Example 4. (trans)-4-Phenyl-L-proline was obtainedin 69% (0.89 gm) yield as white flaky crystals.

EXAMPLE 11 4-Phenyl-1-[(phenylmethoxy)carbonyl]-3,4-dihydro-L-prolinebenzyl ester

Following the procedure as described in Example 3, except substitutingthe Example 7B proline compound for the Example 2 proline compound, thetitle compound is obtained.

EXAMPLE 12 (trans)-4-Phenyl-L-proline

The procedure as described in Example 4 was followed except that theExaple 11 compound was used as the starting material. Thus, a solutionof 2.0 g (0.0048 moles) of the dehydro proline in 20 ml THF was added toa solution of lithium (0.27 g, 0.0387 moles) in ammonia (150 ml) and THF(10 ml) at ˜-78° C. After the addition, the reaction was stirred for 20minutes at -78° C., quenched with 1.0 g of ammonium chloride and workedup using the procedure as in Example 4 to obtain 0.43 g of title product(46%) as white crystals.

EXAMPLE 13 (trans)-4-Cyclohexyl-L-proline hydrochloride

A slurry of (trans)-4-phenyl-L-proline (50 g, 0.262 moles) and platinumoxide (10 g) in absolute ethanol (1200 ml) was treated with 5.62 Nethanolic HCl (46.5 ml, 0.261 moles) and shaken until all the solid hadgone into solution. The solution was then purged with argon andhydrogenated on a Parr apparatus at 50 psi overnight. After this time,the untake of hydrogen had ceased and NMR indicated complete reduction.The reaction mixture was filtered through a pad of Cellite andconcentrated in vacuo. The residue was triturated with diethylether andfiltered to yield 60.0 g of (trans)-4-cyclohexyl-L-proline hydrochlorideas snow white crystals, m.p. 170°-171° C.

EXAMPLE 14 (trans)-4-Cyclohexyl-L-proline

A solution of 2.0 g (0.0062 moles) of dehydro proline (prepared asdescribed in Example 3) in 10 ml THF was added to a solution of lithium(0.65 g, 0.093 moles) in ammonia (150 ml) at ˜-78° C. After theaddition, the reaction mixture was stirred for 20 minutes and thenabsolute ethanol (3.6 ml, 0.062 moles) was added to the reactionmixture. The reaction mixture was stirred at -33° C. for 6 hours andquenched with 2.0 g of ammonium chloride. Ammonia was evaporated and theresidue was acidified to pH=1 using 5% HCl and extracted with ethylacetate (2 x 100 ml). Palladium hydroxide on carbon (20%, 0.25 g) wasadded to the aqueous layer and hydrogen gas was bubbled through thesolution at room temperature for about 3 hours. It was filtered througha celite pad and the filtrate was concentrated and pH was adjusted to6.3 by adding 5% NaOH solution. The precipitated product was filteredthe next day, and vacuum dried to obtain 0.52 g oftrans-4-cyclohexyl-L-proline as white flaky solid.

What is claimed is:
 1. A compound useful in preparing(cis)-4-hydroxy-4-phenyl proline derivatives or (trans)-4-phenyl prolineprepared by the process which comprises reacting cerium trichloride andphenyllithium at a temperature within the range of from about -90° C. toabout -50° C., for a period of from about 0.1 to about 1 hour, whereinthe cerium trichloride is employed in a molar ratio to the phenyllithiumof within the range of from about 0.2:1 to about 0.35:1.
 2. A processfor preparing a compound useful in preparing (cis)-4-hydroxy-4-phenylproline derivatives or (trans)-4-phenyl proline, which comprisesreacting cerium trichloride and phenyllithium at a temperature withinthe range of from about -90° C. to about -50° C., for a period of fromabout 0.1 to about 1 hour, wherein the cerium trichloride is employed ina molar ratio to the phenyllithium of within the range of from about0.2:1 to about 0.35:1.
 3. The process as defined in claim 2 wherein thecerium trichloride is employed in a molar ratio to the phenyllithium ofwithin the range of from about 0.25:1 to about 0.35:1.
 4. The process asdefined in claim 2 wherein the reaction of cerium trichloride andphenyllithium is carried out at a temperature within the range of fromabout -80° C. to about -50° C.
 5. The process as defined in claim 4wherein the reaction is carried out for a period of from about 0.2 toabout 1 hour.
 6. The process as defined n claim 4 wherein the reactionis carried out in the presence of an inert organic solvent.